http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110452151-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-20 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-20 |
| filingDate | 2019-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2022-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2022-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-110452151-B |
| titleOfInvention | A kind of synthetic method of α-indole glycine derivative |
| abstract | The invention discloses a synthesis method of α-indole glycine derivatives. The synthesis method uses glycine derivatives and substituted indole as raw materials, acetonitrile as solvent, and organic dye Rose Bengal as photosensitive catalyst. Under air conditions, the corresponding indole glycine derivatives were synthesized in one step by light irradiation. The synthetic method of the present invention is green and environment-friendly, does not need to use toxic catalysts, and the catalysts used at the same time are cheap and the dosage is very low, thereby effectively reducing the production cost; secondly, the operation is convenient, without heating and inert gas protection, and only needs to be heated at room temperature, in the air, The reaction can be carried out under light conditions, and can be applied to large-scale production; finally, the yield of the target compound is high and the substrate range is wide. |
| priorityDate | 2019-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 38.